Astrocytes expressing ALS‐linked mutant FUS induce motor neuron death through release of tumor necrosis factor‐alpha

• Published in: Glia Vol. 66; no. 5; pp. 1016 - 1033
• Main Authors: Kia, Azadeh, McAvoy, Kevin, Krishnamurthy, Karthik, Trotti, Davide, Pasinelli, Piera
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.05.2018; John Wiley and Sons Inc
• Subjects: AMPA receptor; Amyotrophic lateral sclerosis; Amyotrophic Lateral Sclerosis - genetics; Amyotrophic Lateral Sclerosis - metabolism; Animals; Antibodies; Astrocytes; Astrocytes - metabolism; Astrocytes - pathology; Axons; Cell death; Cell Death - physiology; Cells, Cultured; Coculture Techniques; Conditioning; Culture Media, Conditioned; cytokine; Degeneration; Excitotoxicity; FUS protein; Gliosis; Gliosis - pathology; Humans; Inflammation; Inflammatory response; Mice; Mortality; Motor neurons; Motor Neurons - metabolism; Motor Neurons - pathology; Mutation; Necrosis; Neurites - metabolism; Neurites - pathology; Neurodegeneration; Neurons; NF-kappa B - metabolism; Rats; Receptors; Receptors, AMPA - metabolism; RNA-Binding Protein FUS - genetics; RNA-Binding Protein FUS - metabolism; Sarcoma; Spinal Cord - metabolism; Spinal Cord - pathology; Therapeutic applications; Toxicity; Tumor Necrosis Factor-alpha - metabolism; Tumor necrosis factor-TNF; Tumor necrosis factor-α; α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid; α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors; cytokine; neurodegeneration; AMPA receptor; excitotoxicity
• ISSN: 0894-1491; 1098-1136
• DOI: 10.1002/glia.23298

Mutations in fused in sarcoma (FUS) are linked to amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease affecting both upper and lower motor neurons. While it is established that astrocytes contribute to the death of motor neurons in ALS, the specific contribution of mutant FUS (mutFUS) through astrocytes has not yet been studied. Here, we used primary astrocytes expressing a N‐terminally GFP tagged R521G mutant or wild‐type FUS (WTFUS) and show that mutFUS‐expressing astrocytes undergo astrogliosis, damage co‐cultured motor neurons via activation of an inflammatory response and produce conditioned medium (ACM) that is toxic to motor neurons in isolation. Time lapse imaging shows that motor neuron cultures exposed to mutFUS ACM, but not WTFUS ACM, undergo significant cell loss, which is preceded by progressive degeneration of neurites. We found that Tumor Necrosis Factor‐Alpha (TNFα) is secreted into ACM of mutFUS‐expressing astrocytes. Accordingly, mutFUS astrocyte‐mediated motor neuron toxicity is blocked by targeting soluble TNFα with neutralizing antibodies. We also found that mutant astrocytes trigger changes to motor neuron AMPA receptors (AMPAR) that render them susceptible to excitotoxicity and AMPAR‐mediated cell death. Our data provide the first evidence of astrocytic involvement in FUS‐ALS, identify TNFα as a mediator of this toxicity, and provide several potential therapeutic targets to protect motor neurons in FUS‐linked ALS. Main Points Expression of ALS‐linked Fused in Sarcoma (FUS) R521G variant in astrocytes drives changes which promote motor neuron death. We identify astrocytic NFkB activity, TNFα production and motor neuron AMPARs as mediators of this process.